HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Hydroxide → methyl (7S)-7-[(1-benzylpyrrolidin-2-yl)methoxy]-14-cyclohexyl-7,8-dihydro-6H-indolo[1,2-e][1,5]benzoxazocine-11-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | methyl (7S)-14-cyclohexyl-7-hydroxy-7,8-dihydro-6H-indolo[1,2-e][1,5]benzoxazocine-11-carboxylate | HCID 66674899 | — |
| Reactant | 1-Benzyl-2-(chloromethyl)pyrrolidinium chloride | HCID 86627903 | — |
| Catalyst | Tetrabutylammonium Bromide | HCID 74236 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | methyl (7S)-7-[(1-benzylpyrrolidin-2-yl)methoxy]-14-cyclohexyl-7,8-dihydro-6H-indolo[1,2-e][1,5]benzoxazocine-11-carboxylate | HCID 67344945 | 80% |
Reaction Steps
Methyl (7S)-14-cyclohexyl-7-hydroxy-7,8-dihydro-6H-indolo[1,2-e][1,5]benzoxazocine-11-carboxylate (prepared as described in International patent application WO2006/046030) in toluene (0.17 M) was treated with 30% NaOH (aq) (10 eq) and tetrabutylammonium bromide (0.25 eq). The solution was stirred at RT for 30 min, then 1-benzyl-2-(chloromethyl)pyrrolidinium chloride (2.5 eq) was added to the solution and the resulting mixture was stirred at 60° C. over night. Toluene was eliminated in vacuo; the residue was taken up in EtOAc and washed with 1 N HCl (aq), brine, before being dried (Na2SO4), filtered and concentrated in vacuo. The crude material was purified by FC (PE/EtOAc 50:50+1% NEt3) to afford the product (80%). (ES+) m/z 579 (M+H)+
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07989438B2 |
| Source dataset | uspto-grants-2011_08 |
| ORD ID | ord-dd6b5182eece4c71b16dfad9420ccda1 |
| Source note | uspto-grants-2011_08 |